Company ยท US
Cui Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1991. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 30, 1991 | K913140 | SILICONE GEL SHEETING Cui Corp. | MDA |
| Nov 26, 1990 | K904350 | CUI DORSAL COLUMELLA PROSTHESIS Cui Corp. | FZE |
| Nov 26, 1990 | K904349 | CUI CURVILINEAR SILICONE CHIN Cui Corp. | FWP |
| Nov 26, 1990 | K904348 | CUI FEATHERED SILICONE MALAR Cui Corp. | LZK |
| Sep 10, 1990 | K903329 | CUI ANATOMICAL SILICONE MALAR Cui Corp. | LZK |
| Sep 10, 1990 | K903328 | CUI PREMAXILLARY IMPLANT Cui Corp. | FZE |
| Sep 10, 1990 | K903327 | CUI ARTICULATED SILICONE CHIN Cui Corp. | FWP |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||